Skip to main content
Top
Published in: Familial Cancer 2/2020

01-04-2020 | Colorectal Cancer | Original Article

Detection of DNA mismatch repair deficient crypts in random colonoscopic biopsies identifies Lynch syndrome patients

Authors: Randall E. Brand, Beth Dudley, Eve Karloski, Rohit Das, Kimberly Fuhrer, Rish K. Pai, Reetesh K. Pai

Published in: Familial Cancer | Issue 2/2020

Login to get access

Abstract

The hallmark of Lynch syndrome (LS)-associated neoplasia is DNA mismatch repair protein (MMR) deficiency. Recent studies have demonstrated that histologically normal colonic crypts in patients with LS can exhibit deficient MMR expression. The aim of this study was to determine the feasibility of detecting MMR deficient crypts in random colonoscopic biopsies of normal mucosa in patients with and without LS. Forty-nine patients, including 33 with LS, 12 without LS, and 4 with germline MMR gene variants of uncertain significance (VUS), were prospectively and blindly evaluated by immunohistochemistry for MMR deficient crypts within random normal-appearing mucosal biopsies obtained during surveillance colonoscopy. MMR deficient crypts were identified in 70% (23/33) of patients with LS and in no patients without LS (0/12) (p < 0.001). MMR deficient crypts were identified with nearly equal frequency in both LS patients with and without a cancer history and were associated with germline variants in all four MMR genes and EPCAM. MMR deficient crypts were also identified in LS patients with a history of non-colorectal cancer types, including patients with endometrial cancer, skin sebaceous neoplasms, and renal cancer. Two of the four patients with germline MMR gene VUS had MMR deficient crypts. In conclusion, MMR deficient crypts are a specific biomarker of LS and can be identified in random normal mucosal biopsies in LS patients. Evaluation for MMR deficient crypts in colonoscopic biopsies of normal mucosa can help identify LS patients.
Literature
1.
go back to reference Ladabaum U, Ford JM, Martel M et al (2015) American Gastroenterological Association technical review on the diagnosis and management of Lynch syndrome. Gastroenterology 149:783–813CrossRef Ladabaum U, Ford JM, Martel M et al (2015) American Gastroenterological Association technical review on the diagnosis and management of Lynch syndrome. Gastroenterology 149:783–813CrossRef
2.
go back to reference Evaluation of Genomic Applications in Practice, Prevention Working Group (2009) Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. Genet Med 11:35–41CrossRef Evaluation of Genomic Applications in Practice, Prevention Working Group (2009) Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. Genet Med 11:35–41CrossRef
3.
go back to reference Giardiello FM, Allen JI, Axilbund JE et al (2014) Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on colorectal cancer. Gastroenterology 147:502–526CrossRef Giardiello FM, Allen JI, Axilbund JE et al (2014) Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on colorectal cancer. Gastroenterology 147:502–526CrossRef
4.
go back to reference Syngal S, Brand RE, Church JM et al (2015) ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes. Am J Gastroenterol 110:223–262CrossRef Syngal S, Brand RE, Church JM et al (2015) ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes. Am J Gastroenterol 110:223–262CrossRef
5.
go back to reference Stoffel EM, Mangu PB, Gruber SB et al (2015) Hereditary colorectal cancer syndromes: American society of clinical oncology clinical practice guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines. J Clin Oncol 33:209–217CrossRef Stoffel EM, Mangu PB, Gruber SB et al (2015) Hereditary colorectal cancer syndromes: American society of clinical oncology clinical practice guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines. J Clin Oncol 33:209–217CrossRef
6.
go back to reference Pai RK, Dudley B, Karloski E et al (2018) DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome. Mod Pathol 31:1608–1618CrossRef Pai RK, Dudley B, Karloski E et al (2018) DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome. Mod Pathol 31:1608–1618CrossRef
7.
go back to reference Kloor M, Huth C, Voigt AY et al (2012) Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study. Lancet Oncol 13:598–606CrossRef Kloor M, Huth C, Voigt AY et al (2012) Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study. Lancet Oncol 13:598–606CrossRef
8.
go back to reference Staffa L, Echterdiek F, Nelius N et al (2015) Mismatch repair-deficient crypt foci in Lynch syndrome—molecular alterations and association with clinical parameters. PLoS ONE 10:e0121980CrossRef Staffa L, Echterdiek F, Nelius N et al (2015) Mismatch repair-deficient crypt foci in Lynch syndrome—molecular alterations and association with clinical parameters. PLoS ONE 10:e0121980CrossRef
9.
go back to reference Shia J, Stadler ZK, Weiser MR et al (2015) Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case. Fam Cancer 14:61–68CrossRef Shia J, Stadler ZK, Weiser MR et al (2015) Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case. Fam Cancer 14:61–68CrossRef
10.
go back to reference Richards S, Aziz N, Bale S et al (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 17:405–424CrossRef Richards S, Aziz N, Bale S et al (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 17:405–424CrossRef
11.
go back to reference Thompson BA, Spurdle AB, Plazzer JP et al (2014) Application of a 5-tiered scheme for standardized classification of 2360 unique mismatch repair gene variants in the InSiGHT locus-specific database. Nat Genet 46:107–115CrossRef Thompson BA, Spurdle AB, Plazzer JP et al (2014) Application of a 5-tiered scheme for standardized classification of 2360 unique mismatch repair gene variants in the InSiGHT locus-specific database. Nat Genet 46:107–115CrossRef
12.
go back to reference Dudley B, Brand RE, Thull D et al (2015) Germline MLH1 mutations are frequently identified in Lynch syndrome patients with colorectal and endometrial carcinoma demonstrating isolated loss of PMS2 immunohistochemical expression. Am J Surg Pathol 39:1114–1120CrossRef Dudley B, Brand RE, Thull D et al (2015) Germline MLH1 mutations are frequently identified in Lynch syndrome patients with colorectal and endometrial carcinoma demonstrating isolated loss of PMS2 immunohistochemical expression. Am J Surg Pathol 39:1114–1120CrossRef
13.
go back to reference Kalady MF, Kravochuck SE, Heald B et al (2015) Defining the adenoma burden in lynch syndrome. Dis Colon Rectum 58:388–392CrossRef Kalady MF, Kravochuck SE, Heald B et al (2015) Defining the adenoma burden in lynch syndrome. Dis Colon Rectum 58:388–392CrossRef
14.
go back to reference Yurgelun MB, Allen B, Kaldate RR et al (2015) Identification of a variety of mutations in cancer predisposition genes in patients with suspected Lynch syndrome. Gastroenterology 149:604–613CrossRef Yurgelun MB, Allen B, Kaldate RR et al (2015) Identification of a variety of mutations in cancer predisposition genes in patients with suspected Lynch syndrome. Gastroenterology 149:604–613CrossRef
15.
go back to reference Sijmons RH, Greenblatt MS, Genuardi M (2013) Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians. Fam Cancer 12:181–187CrossRef Sijmons RH, Greenblatt MS, Genuardi M (2013) Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians. Fam Cancer 12:181–187CrossRef
16.
go back to reference Drost M, Tiersma Y, Thompson BA et al (2018) A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome. Genet Med 21:1486–1496CrossRef Drost M, Tiersma Y, Thompson BA et al (2018) A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome. Genet Med 21:1486–1496CrossRef
Metadata
Title
Detection of DNA mismatch repair deficient crypts in random colonoscopic biopsies identifies Lynch syndrome patients
Authors
Randall E. Brand
Beth Dudley
Eve Karloski
Rohit Das
Kimberly Fuhrer
Rish K. Pai
Reetesh K. Pai
Publication date
01-04-2020
Publisher
Springer Netherlands
Published in
Familial Cancer / Issue 2/2020
Print ISSN: 1389-9600
Electronic ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-020-00161-w

Other articles of this Issue 2/2020

Familial Cancer 2/2020 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine